(a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules,… — Class II food recall F-1112-2014
Terminated recall by Global Health Laboratories, LLC, reported 2013-12-25, distributed in AZ. The finished dietary supplement product was manufactured with ingredients found to be contaminated with chlora
| Recall number | F-1112-2014 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Global Health Laboratories, LLC, Amityville, NY, United States |
| Recall initiated | 2013-11-07 |
| Classified | 2013-12-18 |
| Reported by FDA | 2013-12-25 |
| Terminated | 2017-03-10 |
| Distributed | AZ |
| UPC / GTIN / UDI-DI | 00014834001096, 00014834001119, 00014834001355 |
| Lot numbers | 1262057, 1262058, 26813, 26813A, 26813B |
Product
(a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules, dietary supplement, Product No. T00135, UPC 0 14834 00135 5; (b) ONEBODE Flo for Family, probiotic enzyme digestive, 360 capsules, dietary supplement, Product No. T00109, UPC 0 14834 00109 6; (c) ONEBODE Flo daily, probiotic enzyme digestive, 6 capsules, dietary supplement (SAMPLE PACK), Product No. T00111, UPC 0 14834 00111 9 --- Mfg. for OneBode, Chandler, Arizona 85226
Reason for recall
The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1112-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.